Assessing ultrastructure of crustacean and insect neuromuscular junctions. 1996

H L Atwood, and R L Cooper
Department of Physiology, University of Toronto, Ontario, Canada. HAROLD@SPINE.MED.UTORONTO.CA

Motor nerve terminals of arthropods provide excellent models for study of synaptic transmission, and their ultrastructure can be investigated in the same endings from which physiological recordings have been obtained. An experimental procedure for marking a recording site for subsequent ultrastructural analysis is described. The most commonly used procedure for ultrastructural analysis has been serial sectioning and three-dimensional reconstruction. This procedure has the advantage of providing information about the entire nerve terminal, including quantitative information on number, sizes, and relative positions of individual synapses and presynaptic 'active zones'. However, several errors may be generated in the process of viewing the sections and making the reconstruction; these errors can in principle lead to overestimation of synapse and active zone size. The errors become relatively more serious for smaller structures. Procedures for alleviating some of the possible errors are outlined. It is desirable to have additional information from other methods, such as freeze-fracture replication, to guide analysis of reconstructions from serial sections. Combined physiological and ultrastructural analysis of arthropod terminals has shown that each terminal has many small synapses, differing in size and in number of active zones, and that in some terminals, many of the observed synapses have a very low probability of transmission when nerve impulses occur at low frequencies.

UI MeSH Term Description Entries
D008854 Microscopy, Electron Microscopy using an electron beam, instead of light, to visualize the sample, thereby allowing much greater magnification. The interactions of ELECTRONS with specimens are used to provide information about the fine structure of that specimen. In TRANSMISSION ELECTRON MICROSCOPY the reactions of the electrons that are transmitted through the specimen are imaged. In SCANNING ELECTRON MICROSCOPY an electron beam falls at a non-normal angle on the specimen and the image is derived from the reactions occurring above the plane of the specimen. Electron Microscopy
D009046 Motor Neurons Neurons which activate MUSCLE CELLS. Neurons, Motor,Alpha Motorneurons,Motoneurons,Motor Neurons, Alpha,Neurons, Alpha Motor,Alpha Motor Neuron,Alpha Motor Neurons,Alpha Motorneuron,Motoneuron,Motor Neuron,Motor Neuron, Alpha,Motorneuron, Alpha,Motorneurons, Alpha,Neuron, Alpha Motor,Neuron, Motor
D009469 Neuromuscular Junction The synapse between a neuron and a muscle. Myoneural Junction,Nerve-Muscle Preparation,Junction, Myoneural,Junction, Neuromuscular,Junctions, Myoneural,Junctions, Neuromuscular,Myoneural Junctions,Nerve Muscle Preparation,Nerve-Muscle Preparations,Neuromuscular Junctions,Preparation, Nerve-Muscle,Preparations, Nerve-Muscle
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D013569 Synapses Specialized junctions at which a neuron communicates with a target cell. At classical synapses, a neuron's presynaptic terminal releases a chemical transmitter stored in synaptic vesicles which diffuses across a narrow synaptic cleft and activates receptors on the postsynaptic membrane of the target cell. The target may be a dendrite, cell body, or axon of another neuron, or a specialized region of a muscle or secretory cell. Neurons may also communicate via direct electrical coupling with ELECTRICAL SYNAPSES. Several other non-synaptic chemical or electric signal transmitting processes occur via extracellular mediated interactions. Synapse

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